Progress of clinical research studies on tuberous sclerosis complex-related epilepsy in China.

Tinghong Liu, Feng Chen, Feng Zhai, Shuli Liang

Journal: Acta neurologica Scandinavica 2023;146(6):743-751

PMID: 36000491

Abstract

Tuberous sclerosis complex (TSC) is an autosomal dominant neurocutaneous syndrome, with 75.6%-83.5% and 54.1% patients presenting with epilepsy and drug-resistant epilepsy (DRE), respectively. Clinical studies on TSC, particularly surgical interventions, have achieved rapid and substantial progress. The TSC-Task Force Committee of the China Association Against Epilepsy (CAAE-TFTSC) was founded in 2012, and annual academic conferences on the surgical treatment of TSC-related epilepsy have been held since 2013. 'China experts' consensus on surgical treatment of TSC-related epilepsy' was published in 2019. This review focuses on surgical treatment, including resective surgery, neuromodulations, corpus callosotomy and mini-invasive ablations, as well as studies on phenotype, genotype and anti-seizure therapies of mammalian target of rapamycin inhibitor, vigabatrin and ketogenic diet in patients with TSC-related DRE in China.

© 2022 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Address: Functional Neurosurgery Department, National Children's Health Center of China, Beijing Children's Hospital, Capital Medical University, Beijing, China.; Key Laboratory of Major Diseases in Children, Ministry of Education, Beijing, China.
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